Evidence map›Paper›PMID 39976088›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025

N4-Acetylcytidine-Mediated CD2BP2-DT Drives YBX1 Phase Separation to Stabilize CDK1 and Promote Breast Cancer Progression.

Hongyu Wang, Bozhi Zhao, Jiayu Zhang, Qunyu Hu, Linlin Zhou, Yinghui Zhang, Yixin Cai, Yuansong Qu, Tao Jiang, Dongwei Zhang

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

  1. Cancer biology & therapy · 2026
    Article
  2. Review
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  8. Functional roles and mechanisms of NAT10-mediated RNA acFrontiers in cell and developmental biology · 2026
    Review
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  10. Article
  11. Review
  12. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Hongyu WangDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Bozhi ZhaoDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Jiayu ZhangDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Qunyu HuDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Linlin ZhouDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Yinghui ZhangDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Yixin CaiDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Yuansong QuDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Tao JiangDepartment of General Surgery, The Affiliated Hospital of Xuzhou Medical University, Institute of Digestive Diseases, Xuzhou Medical University, Xuzhou, 221002, China.
Dongwei ZhangDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.ORCID https://orcid.org/0009-0003-7740-1056

Funding

Cultivation Plan for High level Scientific Research Projects of Xuzhou Medical University Affiliated HospitalNational Natural Science Foundation of ChinaPostgraduate Research & Practice Innovation Program of Jiangsu Province
6 · The paper itself

Abstract

Long noncoding RNAs (lncRNAs) play critical roles in the initiation and progression of breast cancer. However, the specific mechanisms and biological functions of lncRNAs in breast cancer remain incompletely understood. Bioinformatics analysis identifies a novel lncRNA, CD2BP2-DT, that is overexpressed in breast cancer and correlates with adverse clinicopathological features and poor overall survival. Both in vivo and in vitro experiments demonstrate that CD2BP2-DT promotes proliferation of breast cancer cells. Mechanistically, NAT10 mediates the N4-acetylcytidine (ac4C) modification of CD2BP2-DT, enhancing its RNA stability and expression. More importantly, CD2BP2-DT enhances the stability of CDK1 mRNA by mediating YBX1 phase separation, thereby promoting the proliferation of breast cancer cells. In conclusion, the lncRNA CD2BP2-DT is identified as a crucial driver of breast cancer cell proliferation through the YBX1/CDK1 axis, highlighting its potential as a promising biomarker and therapeutic target for breast cancer.

Indexed as

Breast NeoplasmsCDC2 Protein KinaseRNA, Long NoncodingY-Box-Binding Protein 1AnimalsCell Line, TumorCell ProliferationDisease ProgressionFemaleGene Expression Regulation, NeoplasticHumansMiceMice, NudePhase SeparationCDC2 Protein KinaseCDK1 protein, humanRNA, Long NoncodingY-Box-Binding Protein 1YBX1 protein, humanbreast cancerCD2BP2‐DTN4‐acetylcytidinephase separationproliferationYBX1

Identifiers

PMID39976088
PMCPMC12005790

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.